Taiwan FDA registration 756fb069639380e65c97c689de67f55d
"Medtronic" Primor cervical interbody device
TW: “美敦力”普瑞佛頸椎椎體間裝置
Taiwan·Risk Class 2·MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.·Registered Dec 23, 2011 – Dec 23, 2021CancelledRegistration details
- Analysis ID
- 756fb069639380e65c97c689de67f55d
- Customs Code
- DHA00602322205
Company information
- Manufacturer Country
- United States;;Germany
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Dec 23, 2011
- Expiry Date
- Dec 23, 2021
- Cancellation Date
- Oct 12, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Medtronic" Primor cervical interbody device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 756fb069639380e65c97c689de67f55d and manufactured by MEDTRONIC SOFAMOR DANEK DEGGENDORF GMBH;; MEDTRONIC SOFAMOR DANEK USA, INC.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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